Busse Rudi, Edwards Gillian, Félétou Michel, Fleming Ingrid, Vanhoutte Paul M, Weston Arthur H
Institut für Kardiovaskuläre Physiologie, Klinikum der J.W. Goethe-Universität, Frankfurt, Germany.
Trends Pharmacol Sci. 2002 Aug;23(8):374-80. doi: 10.1016/s0165-6147(02)02050-3.
Endothelial cells synthesize and release vasoactive mediators in response to various neurohumoural substances (e.g. bradykinin or acetylcholine) and physical stimuli (e.g. cyclic stretch or fluid shear stress). The best-characterized endothelium-derived relaxing factors are nitric oxide and prostacyclin. However, an additional relaxant pathway associated with smooth muscle hyperpolarization also exists. This hyperpolarization was originally attributed to the release of an endothelium-derived hyperpolarizing factor (EDHF) that diffuses to and activates smooth muscle K(+) channels. More recent evidence suggests that endothelial cell receptor activation by these neurohumoural substances opens endothelial cell K(+) channels. Several mechanisms have been proposed to link this pivotal step to the subsequent smooth muscle hyperpolarization. The main concepts are considered in detail in this review.
内皮细胞可响应各种神经体液物质(如缓激肽或乙酰胆碱)和物理刺激(如周期性拉伸或流体剪切应力)而合成并释放血管活性介质。特征最明确的内皮源性舒张因子是一氧化氮和前列环素。然而,还存在一条与平滑肌超极化相关的额外舒张途径。这种超极化最初归因于内皮源性超极化因子(EDHF)的释放,该因子扩散至平滑肌并激活平滑肌钾离子通道。最近的证据表明,这些神经体液物质激活内皮细胞受体可打开内皮细胞钾离子通道。已经提出了几种机制来将这一关键步骤与随后的平滑肌超极化联系起来。本综述将详细探讨主要概念。